Coenzyme Q10 levels in Prader-Willi syndrome: Comparison with obese and non-obese subjects

被引:30
作者
Butler, MG
Dasouki, M
Bittel, D
Hunter, S
Naini, A
DiMauro, S
机构
[1] Childrens Mercy Hosp & Clin, Sect Med Genet & Mol Med, Kansas City, MO 64108 USA
[2] Univ Missouri, Sch Med, Kansas City, MO 64108 USA
[3] Columbia Univ, New York, NY USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 119A卷 / 02期
关键词
plasma coenzyme Q10; low energy expenditure; simple obesity; Prader-Willi syndrome; fat mass; lean mass;
D O I
10.1002/ajmg.a.10055
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Coenzyme Q10 (CoQ10) is an essential component of the mitochondrial respiratory chain and an important scavenger of reactive oxygen species. Low levels are found in individuals with reduced energy expenditure, cardiac and skeletal muscle dysfunction, and mitochondrial disorders, many of these manifestations are seen in individuals with Prader-Willi syndrome (PWS). In addition, CoQ10 supplementation frequently is given to individuals with this syndrome. To determine if CoQ10 levels are decreased in PWS, we studied plasma CoQ10 levels in 16 subjects with PWS, 13 with obesity of unknown cause, and 15 subjects without obesity but of similar age and compared with body composition. Plasma CoQ10 levels were significantly decreased (P < 0.05), using several statistical approaches in subjects with PWS (0.45 +/- 0.16 mug/ml), compared to subjects without obesity (0.93 +/- 0.56 mug/ml), but not different from subjects with obesity (0.73 +/- 0.53 mug/ml). When plasma CoQ10 was normalized relative to cholesterol, triglyceride, and creatinine levels and fat and lean mass [determined by dual energy X-ray absorptiometry (DEXA)] in the subjects with either PWS or obesity, no significant differences were observed. However, a lower muscle mass was found in the PWS subjects. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:168 / 171
页数:4
相关论文
共 16 条
[1]  
ANGULO M, 1991, Journal of Pediatric Endocrinology, V4, P167
[2]   THE PRADER-WILLI SYNDROME - A STUDY OF 40 PATIENTS AND A REVIEW OF THE LITERATURE [J].
BRAY, GA ;
DAHMS, WT ;
SWERDLOFF, RS ;
FISER, RH ;
ATKINSON, RL ;
CARREL, RE .
MEDICINE, 1983, 62 (02) :59-80
[3]   Prader-Willi syndrome: Clinical and genetic findings [J].
Butler, MG ;
Thompson, T .
ENDOCRINOLOGIST, 2000, 10 (04) :3S-16S
[4]   CLINICAL AND CYTOGENETIC SURVEY OF 39 INDIVIDUALS WITH PRADER-LABHART-WILLI SYNDROME [J].
BUTLER, MG ;
MEANEY, FJ ;
PALMER, CG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) :793-809
[5]   PRADER-WILLI SYNDROME - CURRENT UNDERSTANDING OF CAUSE AND DIAGNOSIS [J].
BUTLER, MG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 35 (03) :319-332
[6]  
Butler MG, 1998, CLIN GENET, V54, P385
[7]   Prader-Willi syndrome: The effect of growth hormone on childhood body composition [J].
Carrel, AL ;
Myers, SE ;
Whitman, BY ;
Allen, DB .
ENDOCRINOLOGIST, 2000, 10 (04) :43S-49S
[8]  
Cassidy S B, 1984, Curr Probl Pediatr, V14, P1
[9]  
DiMauro S, 1999, ITAL J NEUROL SCI, V20, P387
[10]   Growth hormone deficiency in Prader-Willi syndrome [J].
Eiholzer, U ;
Bachmann, S ;
L'Allemand, D .
ENDOCRINOLOGIST, 2000, 10 (04) :50S-56S